What you want to know
For example, the reviewed-versus-unreviewed six-month disability prevalence difference in the target population.
Statistical foundations · estimates and uncertainty
Use the point estimate to describe what was observed and the interval to judge precision, plausible magnitude and what remains uncertain.
Use this when: an output gives you an estimate and a 95% confidence interval.
You will learn: how large the observed effect is, how precise it is and what remains uncertain.
Then choose: the plain-language p-value guide or return to your analysis.
The central idea
First read what was estimated, in what units and in which direction. Then use the interval to see the range of values still reasonably compatible with the data and model.
Helpful first: use the statistical-foundations guide if samples and target populations are new to you.
By the end you can
1 · Estimate and uncertainty
For example, the reviewed-versus-unreviewed six-month disability prevalence difference in the target population.
One best estimate calculated from the available participants, such as a 0.6 percentage-point difference.
It reflects sample size, variability and design under the chosen statistical model.
Across repeated comparable studies, 95% of intervals made this way would contain the true parameter if the assumptions held.
Do not say there is a 95% probability that this already calculated frequentist interval contains the true value. The interval’s reliability is conditional on the design, model and assumptions and does not measure bias.
2 · Description
Among reviewed participants with observed disability, 45 of 200 had disability: 22.5%. The numerator, denominator, outcome definition and six-month time point are part of the estimate. A confidence interval would describe sampling precision; it would not repair missing outcomes or make the cohort representative of every older adult.
3 · Group comparisons
4 · Differences and ratios
| Effect scale | Null value | Shared-cohort reading |
|---|---|---|
| Mean or proportion difference | 0 | No absolute difference between groups. |
| Proportion, risk, odds, rate or hazard ratio | 1 | The numerator group has the same relative quantity as the reference group. |
The point estimate suggests six-month disability prevalence was 1.03 times as high with review. The interval is compatible with prevalence 24% lower through to 40% higher. It includes 1 and is too wide to establish equivalence.
5 · Regression
After the pre-specified adjustment, the reviewed group had an estimated 36% lower odds of disability. The interval is compatible with substantially lower odds through to almost no difference. It is conditional on the model, covariates, functional forms, analysis population and assumptions. Odds are not risks, and adjustment does not automatically create a causal effect.
Name the outcome, model, reference group, covariates, analysis population and how the interval was calculated.
Report the estimate and 95% CI with units or effect scale, then the p-value if it serves a planned test.
Compare the compatible range with clinical importance and explain bias, confounding and assumption limits.
6 · A fixed reading order
Prevalence, mean difference, odds ratio, rate ratio or another named estimand.
State numerator, comparator and coding.
Translate it into medically intelligible language.
State the range of effects compatible with the data and model.
They answer different questions.
Precision is not validity and association is not automatically causation.
Reading this result in a paper? Use the paper-appraisal guide to keep the estimate with the study design, denominators, bias and relevance.
7 · Beginner self-check
No. State the point estimate and the full compatible range. Inclusion of the null is not proof of no association or equivalence.
No. More information may narrow the interval around the same biased estimate. Design, measurement and causal adjustment determine validity.
Yes. A precise estimate may concern a trivial effect, the wrong target population or a biased comparison. Precision is only one part of interpretation.
Optional authoritative sources for interval estimation, interpretation and reporting.
A clinically framed introduction to uncertainty and interval interpretation.
Open the BMJ chapterGuidance on effect estimates, imprecision, clinical importance and cautious conclusions.
Open Cochrane Handbook chapter 15International principles for estimates, uncertainty, hypotheses and confirmatory analysis.
Open the guidelineUse the standard matched to the medical-study design and analytical purpose.
Open EQUATOR